CROs
Participant Recruitment
Does the IRB need to approve doctor-to-doctor letters?
Blog Posts
Regulatory Compliance
What are the IRB review requirements for human factors/usability testing?
Blog Posts
Clinical Trial Safety
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
Clinical Endpoints
A Successful DMC Requires a Productive, Early Organizational Meeting
Blog Posts
WCG’s Virgil Investigative Study Platform
Solution Overviews
Cell & Gene Therapy
WCG IRB’s Response to COVID-19 in 2020: Supporting the Clinical Trial Industry When It Needed It the Most
Case Studies
Clinical Endpoints
CNS Trial Failure Rates High As Need for New Drugs Grows
Blog Posts
Clinical Endpoints
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Whitepapers
Clinical Endpoints
Can Your ePRO for Pediatric Clinical Trials Support Multiple Informants?
Blog Posts
Clinical Endpoints